Cognitive behavioral therapy for insomnia in stable heart failure: Protocol for a randomized controlled trial |
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Affiliation: | 1. Yale School of Nursing, 400 West Campus Drive, West Haven, CT 06477, United States;2. Penn State Milton S. Hershey Medical Center, 500 University Drive, Hershey, PA 17033, United States;3. Yale School of Medicine, 333 Cedar Street, New Haven, CT 06510, United States;1. Duke University, Duke Clinical Research Institute, Durham, NC, United States;2. Ruhr University Bochum, Bad Oeynhausen, Germany;3. Thomas Jefferson University, Philadelphia, PA, United States;4. ResMed Science Center, ResMed Corp., San Diego, CA, United States;5. Johns Hopkins University, Baltimore, MD, United States;6. Vanderbilt University, Nashville, TN, United States;7. Inova Heart and Vascular Institute, Falls Church, VA, United States;1. Center for Clinical Research Västerås, Uppsala University, Västerås, Sweden;2. Department of Medicine, Västmanland County Hospital Västerås, Västerås, Sweden;1. Section of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT;2. Yale School of Nursing, West Haven, CT;3. Section of Geriatrics, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT |
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Abstract: | BackgroundChronic insomnia is associated with disabling symptoms and decrements in functional performance. It may contribute to the development of heart failure (HF) and incident mortality. In our previous work, cognitive-behavioral therapy for insomnia (CBT-I), compared to HF self-management education, provided as an attention control condition, was feasible, acceptable, and had large effects on insomnia and fatigue among HF patients.ObjectivesThe purpose of this randomized controlled trial (RCT) is to evaluate the sustained effects of group CBT-I compared with HF self-management education (attention control) on insomnia severity, sleep characteristics, daytime symptoms, symptom clusters, functional performance, and health care utilization among patients with stable HF. We will estimate the cost-effectiveness of CBT-I and explore the effects of CBT-I on event-free survival (EFS).MethodsTwo hundred participants will be randomized in clusters to a single center parallel group (CBT-I vs. attention control) RCT. Wrist actigraphy and self-report will elicit insomnia, sleep characteristics, symptoms, and functional performance. We will use the psychomotor vigilance test to evaluate sleep loss effects and the Six Minute Walk Test to evaluate effects on daytime function. Medical record review and interviews will elicit health care utilization and EFS. Statistical methods will include general linear mixed models and latent transition analysis. Stochastic cost-effectiveness analysis with a competing risk approach will be employed to conduct the cost-effectiveness analysis.DiscussionThe results will be generalizable to HF patients with chronic comorbid insomnia and pave the way for future research focused on the dissemination and translation of CBT-I into HF settings. |
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